US2152003A - Insecticide and fumigant - Google Patents
Insecticide and fumigant Download PDFInfo
- Publication number
- US2152003A US2152003A US105268A US10526836A US2152003A US 2152003 A US2152003 A US 2152003A US 105268 A US105268 A US 105268A US 10526836 A US10526836 A US 10526836A US 2152003 A US2152003 A US 2152003A
- Authority
- US
- United States
- Prior art keywords
- insecticide
- butadiene
- effective amount
- fungicide
- composition containing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000002917 insecticide Substances 0.000 title description 17
- 239000002316 fumigant Substances 0.000 title description 4
- 230000000855 fungicidal effect Effects 0.000 description 12
- 230000000844 anti-bacterial effect Effects 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 11
- 239000000417 fungicide Substances 0.000 description 10
- UCAOGXRUJFKQAP-UHFFFAOYSA-N n,n-dimethyl-5-nitropyridin-2-amine Chemical compound CN(C)C1=CC=C([N+]([O-])=O)C=N1 UCAOGXRUJFKQAP-UHFFFAOYSA-N 0.000 description 10
- 239000003899 bactericide agent Substances 0.000 description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 239000004593 Epoxy Substances 0.000 description 6
- 150000002924 oxiranes Chemical class 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 241000282414 Homo sapiens Species 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 230000000749 insecticidal effect Effects 0.000 description 3
- 241001674044 Blattodea Species 0.000 description 2
- 241000254173 Coleoptera Species 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
- APXNRLPBXNJAGG-UHFFFAOYSA-N 1,2:3,4-diepoxycyclohexane Chemical compound C1CC2OC2C2OC12 APXNRLPBXNJAGG-UHFFFAOYSA-N 0.000 description 1
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 description 1
- ITMIRWIISVVMAK-UHFFFAOYSA-N 2-chloro-3-ethyloxirane Chemical compound CCC1OC1Cl ITMIRWIISVVMAK-UHFFFAOYSA-N 0.000 description 1
- 229910014033 C-OH Inorganic materials 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229910014570 C—OH Inorganic materials 0.000 description 1
- ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 description 1
- GXBYFVGCMPJVJX-UHFFFAOYSA-N Epoxybutene Chemical compound C=CC1CO1 GXBYFVGCMPJVJX-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 description 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical compound [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/20—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom three- or four-membered rings
Definitions
- An insecticide, fungicide and batericide composition containing an effective amount of butadiene monoxide.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL2152003X | 1935-10-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2152003A true US2152003A (en) | 1939-03-28 |
Family
ID=19873750
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US105268A Expired - Lifetime US2152003A (en) | 1935-10-29 | 1936-10-12 | Insecticide and fumigant |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US2152003A (en)) |
| FR (1) | FR812749A (en)) |
| NL (1) | NL43500C (en)) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2432118A (en) * | 1944-01-07 | 1947-12-09 | Geigy Ag J R | Chlorophenyl glycidic acid ester insecticides |
| US2676131A (en) * | 1948-12-04 | 1954-04-20 | Shell Dev | Halogenated heterocyclic insect toxicants |
| US2687406A (en) * | 1951-07-05 | 1954-08-24 | Du Pont | 4-vinylcyclohexene monoepoxide and polymers thereof |
| US2687404A (en) * | 1951-07-05 | 1954-08-24 | Du Pont | Epoxy-containing copolymers of 4-vinylcyclohexene monoepoxide and a polymerizable ethylenically unsaturated compound |
| US2785185A (en) * | 1952-08-07 | 1957-03-12 | Union Carbide & Carbon Corp | Process for making oxirane compounds from olefins and aldehyde monoperacylates |
| US2894959A (en) * | 1956-12-17 | 1959-07-14 | Union Carbide Corp | 4,5-epoxycyclohexane-1,2-dicarbonitriles and process of preparing the same |
| US3215738A (en) * | 1962-01-24 | 1965-11-02 | Hoffmann La Roche | N-(substituted-phenethyl)-1-hydroxy-1-cycloalkyl-ethylamines |
| US3261874A (en) * | 1962-08-22 | 1966-07-19 | Exxon Research Engineering Co | Preparation and polymerization of 1,4-pentadiene monoxide |
| US5153229A (en) * | 1990-06-01 | 1992-10-06 | Doyle E. Chastain | Process for producing reference bactericidal endpoint (RBE) limonene |
| WO2005089549A1 (en) * | 2004-03-22 | 2005-09-29 | Valtion Teknillinen Tutkimuskeskus | Use of epoxides as fungicides |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2651579A (en) * | 1946-08-12 | 1953-09-08 | Pennsylvania Salt Mfg Co | Halogenated thiophene pesticide |
| US2600126A (en) * | 1947-05-07 | 1952-06-10 | American Cyanamid Co | Halogenated and nitro halogenated thiophenes as agricultural fungicides |
| US2527372A (en) * | 1948-02-25 | 1950-10-24 | Dow Chemical Co | Diphenyl halo-thiophene and fungicidal compositions containing the same |
| US2690413A (en) * | 1948-09-22 | 1954-09-28 | Socony Vacuum Oil Co Inc | Method of fumigation with acetylated halogenated thiophene |
-
0
- NL NL43500D patent/NL43500C/xx active
-
1936
- 1936-10-12 US US105268A patent/US2152003A/en not_active Expired - Lifetime
- 1936-10-29 FR FR812749D patent/FR812749A/fr not_active Expired
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2432118A (en) * | 1944-01-07 | 1947-12-09 | Geigy Ag J R | Chlorophenyl glycidic acid ester insecticides |
| US2676131A (en) * | 1948-12-04 | 1954-04-20 | Shell Dev | Halogenated heterocyclic insect toxicants |
| US2687406A (en) * | 1951-07-05 | 1954-08-24 | Du Pont | 4-vinylcyclohexene monoepoxide and polymers thereof |
| US2687404A (en) * | 1951-07-05 | 1954-08-24 | Du Pont | Epoxy-containing copolymers of 4-vinylcyclohexene monoepoxide and a polymerizable ethylenically unsaturated compound |
| US2785185A (en) * | 1952-08-07 | 1957-03-12 | Union Carbide & Carbon Corp | Process for making oxirane compounds from olefins and aldehyde monoperacylates |
| US2894959A (en) * | 1956-12-17 | 1959-07-14 | Union Carbide Corp | 4,5-epoxycyclohexane-1,2-dicarbonitriles and process of preparing the same |
| US3215738A (en) * | 1962-01-24 | 1965-11-02 | Hoffmann La Roche | N-(substituted-phenethyl)-1-hydroxy-1-cycloalkyl-ethylamines |
| US3261874A (en) * | 1962-08-22 | 1966-07-19 | Exxon Research Engineering Co | Preparation and polymerization of 1,4-pentadiene monoxide |
| US5153229A (en) * | 1990-06-01 | 1992-10-06 | Doyle E. Chastain | Process for producing reference bactericidal endpoint (RBE) limonene |
| WO2005089549A1 (en) * | 2004-03-22 | 2005-09-29 | Valtion Teknillinen Tutkimuskeskus | Use of epoxides as fungicides |
Also Published As
| Publication number | Publication date |
|---|---|
| NL43500C (en)) | |
| FR812749A (fr) | 1937-05-15 |
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